HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 659099Erstellt: 25. Oktober 2026
2-(Dimethylamino)ethanol → 2-Bromo-6-phenylpyridine
https://huagongshe.com/reaction/659099
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-(Dimethylamino)ethanol | HCID 7902 | — |
| Edukt | Carbon tetrabromide | HCID 11205 | — |
| Edukt | 2-Phenylpyridine | HCID 13887 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Heptane | HCID 8900 | — |
| Produkt | 2-Bromo-6-phenylpyridine | HCID 568679 | — |
Reaktionsschritte
To N,N-dimethylethanolamine (0.8 mL, 8.00 mmol) in heptane (10 mL) cooled externally to 0° C. was added dropwise a 2.5 M n-butyllithium solution (6.40 mL) and the reaction mixture stirred for 30 minutes. 2-Phenylpyridine (12) (412 mg, 2.66 mmol) in heptane (5 mL) was then added and the reaction mixture stirred for a further 1 hour. The reaction was then cooled and carbon tetrabromide (3.18 g, 9.60 mmol) was added whilst maintaining the temperature at −78° C. The reaction was kept at −78° C. for 1 hour and then allowed to warm to ambient temperature. Water was cautiously added and extracted with TBME (×2), dried (Na2SO4) and the solvent concentrated in vacuo. The crude product was purified by column chromatography eluting with 5% EtOAc in heptane to give the title compound. Yield: 300 mg, 48%; LC-MS tr 1.63 min; HPLC Purity: 97%; MS (ES+) m/z 234, 236 (M+H)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08080567B2 |
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| Quelldatensatz | uspto-grants-2011_12 |
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| ORD ID | ord-65c3036df0ef4a609ae2dc80275f93d8 |
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| Quellennotiz | uspto-grants-2011_12 |
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